Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions
Autor: | Yasunori Matsunari, Hideto Matsui, Masaaki Doi, Mitsuhiko Sugimoto, Masahiko Kawaguchi |
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Rok vydání: | 2016 |
Předmět: |
Blood Platelets
0301 basic medicine Cathepsin G Platelet Aggregation Neutrophils 030204 cardiovascular system & hematology Fibrin Thromboplastin Sepsis 03 medical and health sciences Tissue factor chemistry.chemical_compound Platelet Adhesiveness 0302 clinical medicine Von Willebrand factor hemic and lymphatic diseases von Willebrand Factor medicine Humans Platelet Thrombus Whole blood biology Thrombosis Hematology medicine.disease Cell biology 030104 developmental biology chemistry Immunology cardiovascular system biology.protein Blood Flow Velocity circulatory and respiratory physiology |
Zdroj: | International Journal of Hematology. 104:661-668 |
ISSN: | 1865-3774 0925-5710 |
DOI: | 10.1007/s12185-016-2086-z |
Popis: | Von Willebrand factor (VWF) plays an important role in mediating platelet adhesion and aggregation under high shear rate conditions. Such platelet aggregates are strengthened by fibrin-network formation triggered by tissue factor (TF). However, little is known about the role of TF in VWF-dependent thrombus formation under blood flow conditions. We evaluated TF in thrombus formation on immobilized VWF under whole blood flow conditions in an in vitro perfusion chamber system. Surface-immobilized TF amplified intra-thrombus fibrin generation significantly under both low and high shear flow conditions, while TF in sample blood showed no appreciable effects. Furthermore, immobilized TF enhanced VWF-dependent platelet adhesion and aggregation significantly under high shear rates. Neutrophil cathepsin G and elastase increased significantly intra-thrombus fibrin deposition on immobilized VWF-TF complex, suggesting the involvement of leukocyte inflammatory responses in VWF/TF-dependent mural thrombogenesis under these flow conditions. These results reveal a functional link between VWF and TF under whole blood flow conditions, in which surface-immobilized TF and VWF mutually contribute to mural thrombus formation, which is essential for normal hemostasis. By contrast, TF circulating in blood may be involved in systemic hypercoagulability, as seen in sepsis caused by severe microbial infection, in which neutrophil inflammatory responses may be active. |
Databáze: | OpenAIRE |
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